Superfund Proposed Plan
Jackson Steel Site
Mineola/North Hempstead, New York
&EPA
Region 2	July 2004
	
PURPOSE OF PROPOSED PLAN
This Proposed Plan describes the remedial alternatives considered for the
contaminated soil, soil vapor, and groundwater at the Jackson Steel Superfund
site, and identifies the preferred remedy with the rationale for this preference.
The Proposed Plan was developed by the U.S. Environmental Protection Agency
(EPA) in consultation with the New York State Department of Environmental
Conservation (NYSDEC). EPA is issuing this Proposed Plan as part of its public
participation responsibilities under Section 117(a) of the Comprehensive Environ-
mental Response, Compensation, and Liability Act (CERCLA) of 1980, as amended,
and Sections 300.430(f) and 300.435(c) of the National Oil and Hazardous
Substances Pollution Contingency Plan (NCP). The alternatives summarized here
are described in the March 2004 Remedial Investigation/Feasibility Study (RI/FS)1
Report. EPA and the NYSDEC encourage the public to review these documents to
gain a more comprehensive understanding of the site and Superfund activities that
have been conducted at the site.
This Proposed Plan is being provided as a supplement to the RI/FS report to inform
the public of EPA's and NYSDEC's preferred remedy and to solicit public comments
pertaining to all of the remedial alternatives evaluated, including the preferred soil and
groundwater alternatives. EPA's preferred soil and soil vapor remedy consists of in-
situ soil vapor extraction (ISVE)2 for subsurface soils contaminated with volatile
organic compounds (VOCs) and excavation and off-site disposal for the contents of
the dry wells, the trench and sumps inside the building, and surface soils
contaminated with VOCs, semi-volatile organic compounds (SVOCs), pesticides, and
metals. In addition, the building floor would be decontaminated. To address the
contaminated groundwater, EPA's preferred remedy is in-situ chemical treatment of
the contaminated upper aquifer in the source area and extraction and treatment of the
contaminated lower aquifer. In consultation with NYSDEC, the extent of the off-site
groundwater contamination and its potential impact on the public water supply wells
would be determined during the remedial design phase. Based on the evaluation of
off-site groundwater data that would be collected, if it is determined that site-related
contamination is affecting the aquifer, the proposed remedy would be expanded, as
necessary, to include the off-site groundwater contamination and its potential impacts
on the public water supply wells.
The remedy described in this Proposed Plan is the preferred remedy for the site.
Changes to the preferred remedy, or a change from the preferred remedy to another
remedy, may be made if public comments or additional data indicate that such a
change will result in a more appropriate remedial action. The final decision regarding
the selected remedy will be made after EPA has taken into consideration all public
comments. EPA is soliciting public comment on all of the alternatives considered in
the Proposed Plan and in the detailed analysis section of the RI/FS report because
EPA and NYSDEC may select a remedy other than the preferred remedy.
An RI/FS determines the nature and extent of the contamination at and emanating
from a site and identifies and evaluates remedial alternatives.
ISVE involves drawing air through a series of wells to volatilize the solvents in the
soils. The extracted vapors are then treated.
MARK YOUR CALENDAR
July22,2004-August21,2004:
Public comment period on the
Proposed Plan.
August 10, 2004 at 7:00 P.M.:
Public meeting at the Mineola
Village Hall, Gymnasium, 155
Washington Avenue, Mineola, New
York 11501, 516-746-0750.
COMMUNITY ROLE IN SELECTION
PROCESS
EPA and NYSDEC rely on public input
to ensure that the concerns of the
community are considered in selecting
an effective remedy for each
Superfund site. To this end, the RI/FS
report and this Proposed Plan have
been made available to the public for a
public comment period which begins
on July 22, 2004 and concludes on
August 21, 2004.
A public meeting will be held during the
publiccomment period at the Mineola
Village Ha 11 Gymnasium on August 10,
2004 at 7:00 p.m. to present the
conclusions of the RI/FS, to elaborate
further on the reasons for
recommending the preferred remedy,
and to receive public comments.
Comments received at the public
meeting, as well as written comments,
will be documented in the Responsive-
ness Summary Section of the Record
of Decision (ROD), the document
which formalizes the selection of the
remedy.

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Suoerfund Proposed Plan
Jackson Steel Site
	
INFORMATION REPOSITORIES
Copies of the Proposed Plan and supporting docu-
mentation are available at the following information
repositories:
Town of North Hempstead
200 Plandome Road
Manhasset, NY 11030
516-489-5000
Hours: Monday - Friday, 8:15 A.M. - 4:00 P.M.
Garden City Public Library
60 Seventh Street
Garden City, NY 11530
516-742-8405
Hours: Monday - Thursday, 9:30 A.M. - 9:00 P.M.
Friday, 9:30 A.M.-5:30 P.M.
Saturday, 9:00 A.M. - 5:00 P.M.
Sunday, 1:00 P.M. - 5:00 P.M.
Village of Mineola Hall
155 Washington Avenue
Mineola, NY 11501
516-746-0750
Hours: Monday - Friday, 8:30 A.M. - 4:00 P.M.
USEPA-Region II
Superfund Records Center
290 Broadway, 18th Floor
New York, New York 10007-1866
(212) 637-4308
Hours: Monday - Friday, 9:00 A.M. - 5:00 P.M.
Written comments on this Proposed Plan should be
addressed to:
Joel Singerman, Chief
Central New York Remediation Section
U.S. Environmental Protection Agency
290 Broadway, 20th Floor
New York, New York 10007-1866
Telefax: (212)637-3966
Internet: singerman.joel@epa.gov
SCOPE AND ROLE OF ACTION
The primary objectives of this action are to remediate the
source of contamination at the site, reduce and minimize the
potential for soil vapor intrusion, reduce and minimize the
downward migration of contaminants to the aquifer, restore
groundwaterquality, and minimize any potential future health
and environmental impacts.
SITE BACKGROUND
Site Description
The site includes a parcel of property located at 435 First
Street in Mineola, North Hempstead, Nassau County, New
York in a residential/light commercial area. (See Figure 1
for a site plan.) The 1,5-acre property contains a one-story
43,000-square-foot former metal-forming facility and an
approximately 10,000-square foot paved parking area. The
building consists of two sections—the original building,
constructed in 1959, is located closest to First Street, and
the back section, which was added in 1963. The former
office space is located along the north wall, and a loading
dock is located in the southwest corner of the front section
of the building. The building is currently inactive and
predominantly empty, except for miscellaneous small
equipment and supplies abandoned by interim tenants of the
building. An old vertical aboveground storage tank—possibly
used to store degreasing substances—is situated in the
front section of the building next to the former offices. A
trench is located in the floor along the inside western wall of
the building extension, above which a degreasing station is
suspected to have been located. Two sumps are located in
the front section of the building behind the former office
space. One sump is located under the heater and the other
one is located along the eastern wall of the main building.
A third sump is located outside the building, near the main
entrance.
A fence extends along the southern border of the parking
area and separates the Jackson Steel site from the adjacent
former billiards parlor. A narrow strip of unpaved soil is also
located along the east wall of the building, between the
building and the wooden fence separating the Jackson Steel
property from the adjacent apartment complex.
Subsurface features include two dry wells designed to
collect stormwater runoff located under the parking area to
the west of the building and a third dry well is located under
the loading dock area.
The site is bordered to the north by residential, single-family
dwellings, to the east by multiple-family dwellings in a two-
story apartment complex, to the south by the former billiards
parlor and a building that housed a daycare center until April
2002, and to the west by an office building and restaurant
and the predominantly commercial properties along Herricks
Road.
The local topography surrounding the site consists of
relatively flat terrain, with gentle changes in elevation that
typically do not exceed twenty feet of vertical relief. The site
itself is flat with no discernable change in topography, and
has an elevation of 146-148 feet above mean sea level.
EPA Region II - July 2004
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Superfund Proposed Plan
Jackson Steel Site


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Figure 1-Jackson Steel Site Plan
EPA Region II - July 2004
Source: Rettew Associates, Inc.
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Suoerfund Proposed Plan
Jackson Steel Site
Village of Mineola supply well #4 and Garden City Village
supply well #12 are located within a half-mile radius of the
site (east-southeast or sidegradient of the property).
There are no private wells in the area. Area residents utilize
municipal water.
The property, which has been used for industrial/commercial
purposes since it was constructed, has been zoned for a
number of different uses through the past several decades.
The property is presently zoned B-1 for business use as
retail or office space. According to the Village of Mineola's
Department of Planning and Development, it is not
anticipated that the land use will change in the future.
Site Geoloav/Hvdrogeoloav
Surface soils at the site are Upper Pleistocene Deposits,
which are commonly referred to by the name of the
hydrogeologic unit that they form, the Upper Glacial Aquifer.
This Upper Glacial unit consists, predominantly, of varying
consistencies of intermixed-to-interbedded, brown-orange-
yellow sands and gravels to a depth of approximately 105
feet bgs. Some silts were observed, mainly near the ground
surface, but also in smaller quantities deeper in the
formation and in minor lenses throughout. Little or no clay
was observed.
Groundwater beneath the site occurs within the overburden
silty sand of the Upper Glacial Aquifer. The depth to
groundwater is approximately fifty feet bgs.
At approximately 105 feet bgs, the top of the Magothy
Formation is encountered. The top of the formation (the
Magothy Confining Bed) consists of characteristic fine-to-
medium sands interbedded with clay and sandy-silty clay,
with gray coloration, and the presence of organic lignite
(wood) fragments. The Magothy Confining Bed appears to
be a localized occurrence overlying the Magothy Aquifer in
the vicinity of the Jackson Steel site. Its observed thickness
at the site was approximately 296 feet. This thickness
decreases significantly over a relatively short lateral distance
to the northeast (approximately 600 feet) to 42 feet thick. Its
thickness decreases to approximately 167 feet
approximately 600 feet southwest of the site.
The silty clay of the Magothy Confining Bed is believed to be
a semi-confining layer effectively separating the Upper
Glacial Aquifer and the Magothy Formation.
The groundwater flow in the Upper Glacial and Magothy
Aquifers is to the southwest.
Property History
The property was used from the mid-1970s until 1991 as a
"roll form metal shapes" manufacturing facility. Degreasers,
including tetrachloroethylene (PCE), trichloroethylene (TCE),
and 1,1,1-trichloroethane (TCA), were used at the facility
until 1985. Sludges from degreasing equipment were stored
in drums and in an on-site 275-gallon tank.
The analytical results from samples collected by the Nassau
County Department of Health in the early 1990s from within,
around, and below three on-site dry wells indicated the
presence of PCE, TCE, 1,1,1-TCA, 1,2-dichloroethylene
(DCE), and 1,1-dichloroethane (DCA) at depths down to 40
feet below the ground surface. PCE, TCE, 1,1,1-TCA,
1,2-DCE, and 1,1-DCA were also detected in groundwater
samples collected from monitoring wells located
downgradient of the dry wells.
Dumping of wastes into the dry wells, spills, and leaks
during the facility's operations and from drums storing
various chemicals are the likely sources of the
contamination found at the site.
In October 1999, the site was proposed for placement on
EPA's Superfund National Priorities List (NPL). On
February 4, 2000, the site was listed on the NPL.
EPA initiated a search to identify Potentially Responsible
Parties (PRPs) in January 2000. Viable PRPs have not
been found.
Following commencement of field work in October 2001,
because of concerns about the proximity of the site to a
daycare center, the Nassau County Health Department
performed airsampling inside the building. The airsamples
detected PCE at levels below the Health Department's
guideline for indoor PCE exposure. The levels were also
within EPA's acceptable cancer and non-cancer risk ranges.
Given the sensitivity of the population exposed (preschool
children), the Health Department collected additional
samples in mid-December 2001. At that time, indoor testing
was also conducted inside the Jackson Steel building and
a restaurant located adjacent to the site. The results, which
were received in mid-January 2002, indicated that PCE
levels in the indoor air of several rooms in the daycare
facility were above the Health Department's guideline for
indoor PCE exposure. In addition, the maximum level
exceeded EPA's acceptable non-cancer risk level. Low
levels of PCE were detected in the air samples from the
Jackson Steel building and the restaurant. After receiving
the daycare center's results, EPA's emergency response
team installed a vacuum extraction system under the
concrete slab of the building to prevent any contaminants
from entering the building in case the soil and groundwater
under the building are the source. In addition, in order to
provide fresh air circulation in the building, a ventilation
system was installed by the daycare center's contractor.
Samples taken to assess the effectiveness of the above
measures showed that the PCE levels in the air were
significantly below the New York State Health Department
guideline and below EPA's acceptable non-cancer risk
levels.
Because elevated PCE levels were detected in a billiards
club which shared common walls with the Jackson Steel site
EPA Region II - July 2004
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Suoerfund Proposed Plan
Jackson Steel Site
building and the former daycare facility, EPA installed a
vacuum extraction system under the concrete slab of the
billiards club building. Also, a ventilation system was
installed.
RESULTS OF THE REMEDIAL INVESTIGATION
Sampling for the Rl was conducted from October 2001 to
August 2002. The results of the Rl are summarized below.
Soil
Soils at the Jackson Steel site were sampled at 33 locations.
Ten of these locations were situated in unpaved areas
(samples at these locations were collected from shallow
depths). The remaining 23 sampling locations were situated
under the pavement (samples in these areas were collected
at various depths extending to the bottom of the Upper
Glacial Aquifer).
Although VOCs were found at all ten unpaved sampling
locations and all of the 23 soil boring locations, with the
exception of the samples collected near the dry wells, all of
the concentrations exceeding the New York State Technical
and Administrative Guidance Memorandum No. 94-HWR-
4046 (TAGM) objectives1 were found within the top 1 foot of
soil. In the shallow soil, TCE and PCE concentrations
exceeded the TAGM objective at three locations-soil located
near the back door to the building extension and two soil
boring locations within the trench in the building. The
maximum concentrations of TCE and PCE detected at these
three locations were 1,400 and 19,000 micrograms per
kilogram (|jg/kg), respectively. (The TAGM objectives for
TCE and PCE are 700 and 1,400 |jg/kg, respectively.)
Acetone also exceeded the TAGM objective (200 |jg/kg) in
shallow soil samples collected within the unpaved soil areas.
The maximum detected concentration of acetone was 2,000
Mg/kg.
The dry wells are the only locations where VOCs were found
in soil at depths greater than one foot. The sampling results
for the dry wells suggest that it is possible that workers
dumped chemicals containing VOCs into the dry wells.
Although some of the VOC concentrations found in the dry
wells exceeded their TAGM objectives, the concentrations
are much lower in comparison to the concentrations
1
Division Technical and Administrative Guidance
Memorandum: Determination of Soil Cleanup Objectives
and Cleanup Levels, Division of Hazardous Waste
Remediation, January 24, 1994.
There are currently no federal or state promulgated
standards for contaminant levels in soils. There are,
however, To-Be-Considereds, one of which is the New
York State TAGM objectives, are being used as the soil
cleanup levels forthis site. TAGM objectives are the more
stringent cleanup level between a human-health
protection value and a value based on protection of
groundwater as specified in the TAGM. All of these levels
fall within EPA's acceptable risk range.
EPA Region II - July 2004
measured in the dry wells during previous investigations.
The VOCs that exceeded the TAGM objectives and their
maximum concentrations and TAGM objectives are total
xylenes (5,900 |jg/kg; TAGM objective 1,200 |jg/kg), 1,1-
DCA (1,600 |jg/kg; TAGM objective 200 |jg/kg), and 1,1,1-
TCA (1,400 |jg/kg; TAGM objective 800 |jg/kg). In addition,
1,2-cis-DCE, forwhich no TAGM value exists, was detected
at a maximum concentration of 12,000 |jg/kg.
SVOCs, in particular Polynuclear Aromatic Hydrocarbons
(PAHs)2, were found at many of the sampled locations.
PAHs exceeded the TAGM objectives at all ten unpaved soil
sampling locations and at seven of the 23 soil boring
locations sampled for SVOCs. However, with the exception
of the three dry wells and one soil boring, all of the
concentrations exceeding the TAGM objective were found
within the top one foot of soil bgs. Chrysene was the PAH
detected at the highest concentration (5,200 |jg/kg; TAGM
objective 400 |jg/kg), followed by benzo(b)fluoranthene
(5,100 |jg/kg; TAGM objective 1,100 |jg/kg).
PAH contamination in the dry wells appears to be limited to
the top several feet of soil in the dry wells. PAHs tend to
bind more to soil particles than VOCs. This would limit their
vertical leaching and migration through the soil column.
Hence their absence at greater depths in the dry wells. It is
possible that the PAHs found in the top several feet of soil
in the dry wells are the result of sediment washout from the
unpaved soil strips to the dry wells. Of note, the same PAHs
were found at concentrations exceeding the TAGM objective
in all of the soil samples collected from the 0-1 foot bgs
depth interval in the unpaved areas of the site from where
the sediment may have been washed into the dry wells.
Chrysene was the PAH detected at the highest
concentration (4,000 |jg/kg; TAGM objective 400 |jg/kg),
followed by benzo(b)fluoranthene (3,600 |jg/kg; TAGM
objective 1,100 |jg/kg).
Pesticides were detected at concentrations above the
TAGM objective at seven of the 10 unpaved soil sampling
locations. The maximum concentration was measured for
alpha chlordane (1,500 |jg/kg; TAGM objective 540 |jg/kg),
followed by gamma chlordane (570 |jg/kg; TAGM objective
540 |jg/kg). The only location where soil at depth greater
than one foot bgs contained pesticide concentrations above
the TAGM objective was in one of the dry wells located
The results for the PAHs should be viewed with caution,
as the PAHs may not be associated with Jackson Steel's
metal forming operations, but rather with the urban nature
of the area where the site is located, the asphalt
pavement covering the site, and the solid waste
management activities and truck traffic on the property
after Jackson Steel ceased its operations. Specifically,
PAHs are formed mainly during incomplete combustion
processes of organic materials such as wood, coal,
mineral oil, and oil-derived products. As such, they are
ubiquitous in urban environments and are found in air,
soil, water, and food. They are contained in motor-
vehicle exhausts both from gasoline and diesel engines
and are present in crude and refined oils; in commercial
products, such as bitumen (asphalt), coal tars, and
pitches; and in industrial wastes such as waste oil.
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Suoerfund Proposed Plan
Jackson Steel Site
underthe parking area. Two pesticides were found with the
maximum concentration measured for gamma chlordane
(1,100 |jg/kg; TAGM objective 540 |jg/kg).
There is no information on whether chemicals containing
pesticides were used in facility operations. Pesticide
contamination appears to be limited to the parking lot area
where operations are known to have taken place in the past.
It is possible that the pesticides were applied directly for pest
control rather than be the result of the facility's metal-
forming operations.
Metal concentrations exceeded the TAGM objectives at all
ten unpaved sampling locations and at six of the 23 soil
boring locations sampled for metals at the site. These six
soil borings are all located within the building. With the
exception of the indoor dry well, all of the samples
containing concentrations above the TAGM objectives were
collected within the top one foot of soil bgs. The
concentrations of arsenic, cadmium, copper, lead, mercury,
and zinc exceeded the TAGM objectives3. Their maximum
concentrations and TAGM objectives are as follows: arsenic
(62.5 milligrams per kilogram [mg/kg]; TAGM objective 12
mg/kg), cadmium (5.1 mg/kg; TAGM objective 1 mg/kg),
copper (257 mg/kg; TAGM objective 50 mg/kg), lead (1,190
mg/kg; TAGM objective 500 mg/kg), mercury (0.8 mg/kg;
TAGM objective 0.2 mg/kg), and zinc (887 mg/kg; TAGM
objective 50 mg/kg).
Finally, several contaminants (including acetone, SVOCs
and metals) were detected in the three building sumps at
concentrations exceeding the TAGM objectives.
Groundwater
Sampling results for the shallow Upper Glacial Aquifer
indicate that chemicals that may have been discharged into
the dry wells during the active life of the facility have resulted
in the contamination of the shallow Upper Glacial Aquifer at
the site. Specifically, the highest total VOC concentrations
were measured in the monitoring wells located immediately
downgradient of the two dry wells located underthe parking
area. These monitoring wells also contained a higher
number of VOCs exceeding the Maximum Contaminant
Levels (MCLs)4 in comparison to the remaining monitoring
wells. VOCs were also found at the middle of the Upper
Glacial Aquifer at the site, though the concentrations were
lower than those measured in the shallow aquifer at this
location. The following VOCs exceeded their MCLs in the
shallow and middle Upper Glacial Aquifer at the site: 1,1-
DCA; cis-1,2-DCE; PCE; 1,1,1-TCA; and TCE.
Four VOCs, cis-1,2-DCE, methyl tertiary butyl ether (MTBE),
toluene, and TCE, were detected in the shallow and middle
Upper Glacial Aquifer upgradient of the site compared to a
total of thirteen VOCs detected in the groundwater in the
area ofthe dry wells at the site (1,1-DCA, cis-and trans-1,2-
DCE, 1,1,1-TCA, TCE, PCE, benzene, chloroethane,
cyclohexane, ethylbenzene, isopropylbenzene, MTBE, and
toluene). All upgradient concentrations were below MCLs
and the concentrations oftwo ofthe four VOCs, cis-1,2-DCE
and TCE, were orders of magnitude (i.e. ten to one
thousand times) lower at the upgradient location than at the
site. From the thirteen VOCs detected at the site, four
exceeded their MCLs (1,1-DCA, cis 1,2-DCE, PCE, and
TCE). The compound detected at the highest concentration
was cis-1,2-DCE at 340 micrograms per liter (|jg/l), followed
by PCE (63 |jg/l). (The MCLs for cis-1,2-DCE and PCE are
both 5 jjg/l.) These results suggest limited upgradient
contributions to the VOC concentrations detected at the site.
Downgradient ofthe site, only two VOCs, MTBE and toluene
(these compounds were also found upgradient ofthe site),
were found in the shallow and middle Upper Glacial
Aquifer5. The concentrations were below the MCLs.
The sampling results for the base of the Upper Glacial
Aquifer indicated a decrease in the VOC concentrations with
depth upgradient of the site, underlying the site, and
downgradient ofthe site. None of the VOCs detected at the
base ofthe Upper Glacial Aquifer exceeded its MCL. The
compound detected at the highest concentration at the base
ofthe Upper Glacial Aquifer was TCE at 2.5 jjg/l, followed
by PCE at 1.4 jjg/l. (The MCLs for both compounds is 5
MQ/I-)
VOCs were also detected in the lower, Magothy Aquifer.
TCE and PCE exceeded the MCLs at a number of sampling
points in this aquifer at depths between approximately 400
and 450 feet. The compound detected at the highest
Metals occur naturally in the environment. The TAGM
objective to which the on-site metal concentrations were
compared are based on the concentrations at which
metals are known to occur naturally in soil in the eastern
United States. Copper, cadmium, chromium, nickel, lead,
and zinc are also known to be associated with iron and
steel works operations and metal finishing. Therefore,
while some of the metals found in on-site soil may be
naturally occurring, others may be the result of past site
operations. As noted, more exceedances ofthe TAGM
objective and higher metal concentrations, in general,
were noted in the dry well located within the building. It is
possible that during the active life ofthe facility, the floor
ofthe building was washed and the water drained to this
dry well, resulting in the metals found in the sediments in
the dry well.
EPA Region II - July 2004
EPA and New York State Department of Health have
promulgated health-based protective MCLs, which are
enforceable standards for various drinking water
contaminants. MCLs ensure that drinking water does not
pose either a short- or long-term health risk.
Of note, in addition to the occurrence of VOCs that are
likely related to Jackson Steel's metal forming operations,
several VOCs (MTBE, benzene, toluene, ethylbenzene,
xylene and isopropylbenzene) were detected that are
typically related to gasoline and fuel contamination. This
contamination could be attributed to site activities after
Jackson Steel ceased operations, when the site was
used for illegal solid waste management. The presence
of MTBE and toluene in the upgradient monitoring well
would also suggest some upgradient contribution to this
contamination.
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Superfund Proposed Plan
Jackson Steel Site
WHAT IS RISK AND HOW IS IT CALCULATED?
A Superfund baseline human health risk assessment is an
analysis of the potential adverse health effects caused by
hazardous substance releases from a site in the absence of
any actions to control or mitigate these under current- and
future-land uses. A four-step process is utilized for
assessing site-related human health risks for reasonable
maximum exposure scenarios.
Hazard Identification: In this step, the COCs at the site in
various media (i.e., soil, groundwater, surface water, and air)
are identified based on such factors as toxicity, frequency of
occurrence, and fate and transport of the contaminants in the
environment, concentrations of the contaminants in specific
media, mobility, persistence, and bioaccumulation.
Exposure Assessment: In this step, the different exposure
pathways through which people might be exposed to the
contaminants identified in the previous step are evaluated.
Examples of exposure pathways include incidental ingestion
of and dermal contact with contaminated soil. Factors
relating to the exposure assessment include, but are not
limited to, the concentrations that people might be exposed
to and the potential frequency and duration of exposure.
Using these factors, a "reasonable maximum exposure"
scenario, which portrays the highest level of human exposure
that could reasonably be expected to occur, is calculated.
Toxicity Assessment: In this step, thetypes of adverse health
effects associated with chemical exposures, and the
relationship between magnitude of exposure and severity of
adverse effects are determined. Potential health effects are
chemical-specific and may include the risk of developing
cancer over a lifetime or other non-cancer health effects,
such as changes in the normal functions of organs within the
body (e.g., changes in the effectiveness of the immune
system). Some chemicals are capable of causing both
cancer and non-cancer health effects.
Risk Characterization: This step summarizes and combines
outputs of the exposure and toxicity assessments to provide
a quantitative assessment of site risks. Exposures are
evaluated based on the potential risk of developing cancer
and the potential for non-cancer health hazards. The
likelihood of an individual developing cancer is expressed as
a probability. For example, a 10"4 cancer risk means a
"one-in-ten-thousand excess cancer risk"; or one additional
cancer may be seen in a population of 10,000 people as a
result of exposure to site contaminants under the conditions
explained in the Exposure Assessment. Current Superfund
guidelines for acceptable exposures are an individual lifetime
excess cancer risk in the range of 10"4to 10"6 (corresponding
to a one-in-ten-thousand to a one-in-a-million excess cancer
risk) with 10"6 being the point of departure. For non-cancer
health effects, a "hazard index" (HI) is calculated. An HI
represents the sum of the individual exposure levels
compared to their corresponding reference doses. The key
concept for a non-cancer HI is that a "threshold level"
(measured as an HI of less than 1) exists below which non-
cancer health effects are not expected to occur.
concentration in the Magothy Aquifer was TCE (200 jjg/l),
followed by PCE (86 jjg/l). (The MCLs for both compounds
is 5 jjg/l.) The highest concentrations of PCE and of TCE
were detected at 454 feet. Degradation products of PCE
and TCE (cis-1,2-DCE and 1,1-DCE) were also detected at
depth but at very low concentrations (less than 3 jjg/l).
The PCE and TCE concentrations detected in the 300 foot-
deep silt and clay confining layer separating the upper from
the lower aquifers were significantly lower than the
concentrations detected at the top of the Upper Glacial
Aquifer or the bottom of the sampled interval (404 to 454
feet below ground surface) of the Magothy Aquifer.
Specifically, the PCE concentrations in the confining layer
ranged from 2.7 to 13 |jg/kg and the TCE concentrations
ranged from 5.9 to 32 |jg/kg. In addition, the concentrations
of cis 1,2-DCE, which was detected at 340 |jg/kg at the top
of the Upper Glacial Aquifer, ranged from 0.26 to 1 |jg/kg.
These sampling results suggest that the VOC contamination
in the groundwater in the upper aquifer and in the confining
layer is a direct result of contamination migrating vertically
downward from the site.
SVOCs were detected in four of the five wells monitoring the
shallow Upper Glacial Aquifer. There is no information on
the use of SVOCs in facility operations. As was noted
above, SVOCs are common in urban environments. For
compounds with established MCLs, the detected
concentrations were below the corresponding MCLs.
Pesticides were detected in all of the monitoring wells in the
Upper Glacial Aquifer. Metals were detected in all of the
wells located in the Upper Glacial Aquifer. The metals
arsenic, iron, and manganese were detected at
concentrations exceeding the federal and state MCLs. The
maximum concentrations of these metals and their MCLs
are arsenic at 13.5 jjg/l (MCL is 10 jjg/l), iron at 66,100 jjg/l
(MCL is 300 jjg/l), and manganese at 7,070 jjg/l (MCL is
300 jjg/l). The following metals are known to be associated
with iron and steel works operations and metal finishing:
copper, cadmium, chromium, nickel, lead, and zinc. While
some of these metals were found in shallow soil above the
TAGM objectives-possibly indicating their occurrence as a
result of site operations—none of these metals with
established MCLs were detected above their MCLs in the
groundwater samples from the Upper Glacial Aquifer.
Building Floor
Building floor wipe samples contained several SVOCs,
pesticides, and metals. The pesticides may be the result of
their application for the purpose of pest control in the
building. The SVOC measured at the highest concentration
was bis (2-ethylhexyl) phthalate at 5.6 jjg/wipe, followed by
di-n-butylpthalate at 2.9 jjg/wipe. The pesticide measured
at the highest concentration was 4,4-DDE (600 jjg/wipe),
followed by4,4-DDD (190 jjg/wipe).
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Soil Gas and Indoor Air Sampling
EPA conducted an investigation in an attempt to determine
the source of the PCE in the former daycare center located
immediately south of the site. The investigation included the
collection of soil gas samples at numerous locations inside
and outside the former daycare building, and several rounds
of indoor air sampling at the former daycare center and
nearby business and residential buildings6.
The results of soil gas surveys indicated the presence of
PCE, TCE, 1,1,1-TCA, cis-1,2-DCE, and 1,1-DCA in soil gas
at the site, with the highest concentrations being located in
the area around the former dry wells. TCE and PCE were
detected at lower concentrations underneath the billiards
parlor located adjacent to the site and the daycare center
buildings.
PCE, TCE, and other VOCs were detected in airsamples. In
general, higher concentrations of chlorinated solvents were
measured in the air samples collected in the daycare
building when the ventilation systems (building and subslab)
were not operational. The types of compounds found at
higher concentrations varied when the ventilation systems
were switched on and off. Some contaminants such as
toluene were detected at higher concentrations when the
ventilation systems were on. This might imply that there is
an external air pollution source.
Although VOCs were found in soils at the Jackson Steel site,
the contaminants, their concentrations, and locations are not
consistent with the elevated VOC concentrations found in
the soil gas and airsamples.
SUMMARY OF SITE RISKS
Based upon the results of the Rl, a baseline risk assessment
was conducted to estimate the risks associated with current
and future property conditions. A baseline risk assessment
is an analysis of the potential adverse human health effects
caused by hazardous-substance exposure in the absence of
any actions to control or mitigate these under current and
future land uses.
The human-health estimates summarized below are based
on current reasonable maximum exposure scenarios and
were developed by taking into account various conservative
estimates about the frequency and duration of an individual's
exposure to the COCs, as well as the toxicity of these
contaminants.
While a screening of ecological considerations lead to the
conclusion that property conditions do not necessitate a
quantitative ecological risk assessment, a qualitative
discussion is included below.
The investigation also included the collection of deep soil
samples from the parking lot located between the
Jackson Steel site and the former daycare center. See
the discussion in the "Soils" section, above.
EPA Region II - July 2004
Human Health Risk Assessment
As was noted above, the current land use of the property is
industrial/commercial, and it is anticipated that the land use
will not change in the future.
The baseline risk assessment began with selecting COCs in
the various media that would be representative of site risks.
Since the area is served by municipal water, it is not likely
that the groundwater underlying the property will be used for
potable purposes in the foreseeable future; however, since
regional groundwater is designated as a drinking water
source, potential exposure to groundwater was evaluated.
The other media that were evaluated included surface and
subsurface soil and soil gas.
COCs in the groundwater include benzene, arsenic, PCE,
TCE, vinyl chloride, and heptachlor. COCs in the surface
soil include PAHs, dieldrin, heptachlor epoxide, PCE, and
TCE. COCs in the subsurface soil include PAHs, arsenic,
dieldrin, TCE, and PCE. COCs in the dust on the building
floor include arsenic and chromium.
The baseline risk assessment evaluated the health effects
which could result from exposure to contaminated media
through ingestion, dermal contact, or inhalation. Since the
site is zoned for industrial/commercial use, the risk
assessment evaluated current and future hazards and risks
to trespassers and industrial/commercial workers.
The results of the baseline risk assessment indicate that in
its current condition, the site does not present hazards or
increased cancer risks to trespassers. Specifically, under
current-use trespassing scenario, the HI is less than 1 and
the cancer risk is 4x10"6 which is within EPA's acceptable
risk range.
The unremediated site may present hazards and increased
cancer risks under potential future industrial and commercial
use scenarios. Under a future industrial or commercial use
scenario, the hazards and cancer risks would be associated
with ingestion of dust from and dermal contact with the
building floor; ingestion, dermal contact and inhalation of
particles of surface soil; and ingestion, dermal contact, and
inhalation of vapors from the groundwater in both the Upper
Glacial and the Magothy aquifers (if the groundwater is
extracted using a well). The risks would be to future utility
and construction workers outside of the building and future
industrial/commercial workers within or outside of the
building.
The total estimated HI value for exposures to the selected
COCs in surface soil and groundwater in the Upper Glacial
and Magothy aquifers via ingestion, dermal contact and
inhalation was 30 for a future indoor industrial/commercial
worker and 23 for a future outdoor industrial/commercial
worker. These hazards are above EPA's guidelines for
acceptable exposures (HI less than 1) and are mainly
associated with the groundwater in the Upper Glacial and
Magothy aquifers. The estimated HI value for exposure to
building floor contaminants via ingestion and dermal contact
was 5.6 for a future indoor industrial/commercial worker,
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Suoerfund Proposed Plan
Jackson Steel Site
which exceeds EPA's guidelines for acceptable exposures
mentioned above.
The total estimated cancer risk for exposures to the selected
COCs in surface soil and groundwater in the Upper Glacial
and Magothy aquifers via ingestion, dermal contact and
inhalation was 7.9x103 for a future indoor
industrial/commercial worker and 7.3x103 for a future
outdoor industrial/commercial worker. These cancer risks
are above EPA's guidelines for acceptable exposures (1x10"
4) and are mainly associated with the groundwater in the
Upper Glacial and Magothy aquifers.
Ecological Risk Assessment
Information from the NYSDEC Bureau of Wildlife indicates
that there are no endangered or threatened plant or animal
species at or in the vicinity of the site. Therefore, EPA
evaluated potential exposure pathways for non-endangered
and non-threatened animal and plant species. Since the
property includes a mostly paved industrial/commercial
facility, there is minimal habitat available for ecological
receptors on the property. Due to the suburban/commercial
setting, the potential for exposure to receptors and
ecological risk is minimal in the area surrounding the
property as well.
Because the main medium of concern is groundwater, and
the depth to the surface of the groundwater is approximately
fifty feet bgs, direct contact with groundwater by ecological
receptors is unlikely. Because there are no wetlands or
surface water bodies on or in the immediate vicinity of the
site, there is no potential for contaminated groundwater to
discharge into surface water. Therefore, groundwater is not
considered to be an exposure pathway for ecological
receptors.
Soil samples did contain VOCs, some of which are present
in concentrations greater than conservative screening
criteria considered protective of soil invertebrate species.
Therefore, there is a potential for an unacceptable risk to
burrowing animals that may come into contact with these
contaminated surface soils (zero to two-foot depth).
Summary of Human Health and Ecological Risks
The results of the risk assessment indicate that the site may
present an unacceptable non-cancer hazard and an
increased cancer risk to a future adult inside industrial
worker and future adult outside industrial worker. The risks
are mainly associated with exposures to groundwater in the
Upper Glacial and Magothy aquifers. Also, a worker
exposed to dust from the building floor represents an
unacceptable cancer risk and non-cancer HI.
Contamination in the surface soil poses a potential
unacceptable risk to burrowing animals that may come into
contact with these soils.
Based upon the results of the Rl and the risk assessment,
EPA has determined that actual or threatened releases of
hazardous substances from the property, ifnot addressed by
the preferred remedy or one of the other active measures
considered, may present a current or potential threat to
human health and the environment.
REMEDIAL ACTION OBJECTIVES
Remedial action objectives are specific goals to protect
human health and the environment. These objectives are
based on available information and standards, such as
applicable or relevant and appropriate requirements
(ARARs), to-be-considered guidance, and site-specific risk-
based levels.
The following remedial action objectives were established
for the site:
Minimize or eliminate contaminant migration from
contaminated soils and dry wells to the
groundwater;
Minimize or eliminate any contaminant migration
from contaminated soils and groundwater to indoor
air;
Restore groundwaterto levels which meet state and
federal standards within a reasonable time frame;
Mitigate the migration of the affected groundwater;
and
Reduce oreliminate any direct contact, ingestion, or
inhalation threat associated with contaminated
soils, soil vapor, contaminated surfaces in the on-
site building, and groundwater.
Soil cleanup objectives will be those established pursuant to
the TAGM guidelines. These levels are the more stringent
cleanup level between a human-health protection value and
a value based on protection of groundwater as specified in
the TAGM. All of these levels fall within EPA's acceptable
risk range.
Groundwater cleanup goals will be the more stringent of the
state or federal promulgated standards.
SUMMARY OF REMEDIAL ALTERNATIVES
CERCLA §121 (b)(1), 42 U.S.C. §9621 (b)(1), mandates that
remedial actions must be protective of human health and the
environment, cost-effective, comply with ARARS, and utilize
permanent solutions and alternative treatment technologies
and resource recovery alternatives to the maximum extent
practicable. Section 121 (b)(1) also establishes a preference
for remedial actions which employ, as a principal element,
treatment to permanently and significantly reduce the
volume, toxicity, or mobility of the hazardous substances,
pollutants and contaminants at a site. CERCLA §121 (d), 42
U.S.C. §9621 (d), further specifies that a remedial action
must attain a level or standard of control of the hazardous
substances, pollutants, and contaminants, which at least
EPA Region II - July 2004
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Superfund Proposed Plan
Jackson Steel Site
attains ARARs under federal and state laws, unless a waiver
can be justified pursuant to CERCLA §121 (d)(4), 42 U.S.C.
§9621 (d)(4).
Detailed descriptions of the remedial alternatives for
addressing the contamination associated with the site can
be found in the FS report. This document presents five soil
remediation alternatives, seven groundwater remediation
alternatives, and three building floor alternatives. To
facilitate the presentation and evaluation of these
alternatives, the FS report alternatives were reorganized to
formulate the remedial alternatives discussed below.
Alternative SC-2: Excavation of Contaminated Soils,
Building Trench, Sumps, and Contents of Dry Wells;
Off-Site Treatment and/or Disposal; and Building
Decontamination
Capital Cost:	$5,299,000
Annual Operation and Maintenance Cost:	0
Present-Worth Cost:	$5,299,000
Construction Time:	6 months
It should be noted that although the FS report evaluated
chemical oxidation for the lower aquifer, this technology is
not being considered for the lower aquifer in this Proposed
Plan because of the uncertainties regarding the application
of this technology to the depths requiring groundwater
remediation at the site (down to 450 feet). Similarly,
although the FS report evaluated bioremediation, this
technology is not considered for either aquifer because of
the uncertainties regarding favorable microbial conditions at
the site.
The construction time for each alternative reflects only the
time required to construct or implement the remedy and
does not include the time required to design the remedy,
negotiate the performance of the remedy with any PRPs, or
procure contracts for design and construction.
The remedial alternatives are:
Source Control Alternatives
Alternative SC-1: No Action
Capital Cost:	$0
Annual Operation and Maintenance Cost:	$0
Present-Worth Cost:	$0
Construction Time:	0 months
The Superfund program requires that the "no-action"
alternative be considered as a baseline for comparison with
theotheralternatives. The no-action remedial alternative for
soil does not include any physical remedial measures that
address the problem of soil contamination at the property.
Because this alternative would result in contaminants
remaining on-property above levels that allow for
unrestricted use and unlimited exposure, CERCLA requires
that the site be reviewed at least once every five years. If
justified by the review, remedial actions may be
implemented to remove, treat, or contain the contaminated
soils.
This remedial alternative includes the excavation of all
source-area soils down to the watertable, the trench and
sumps inside the building, the drywells, and off-site
treatment and/or disposal. In addition, the building floor
would be decontaminated through vacuuming and power
washing. All vacuumed dust and wash water would be
transported for treatment and/or disposal at an off-site
Resource Conservation and Recovery Act (RCRA)-
compliant facility.
The estimated volume of contaminated soil to be excavated
is 32,500 cubic yards (contamination is as deep as 50 feet).
The actual extent of the excavation and the volume of the
excavated material would be based on post-excavation
confirmatory sampling. Shoring of the excavation and
extraction and treatment of any water that enters the
excavation in the source area would be necessary.
The excavated areas would be backfilled with clean fill and
the previously paved areas would be re-paved. All
excavated material would be characterized and transported
for treatment and/or disposal at an off-site RCRA-compliant
facility.
Alternative SC-3: Excavation of Contaminated Surface
Soils, Building Trench, Sumps, and Contents of Dry
Wells; Off-Site Treatment and/or Disposal; Treatment of
VOC-Contaminated Subsurface Soils Using ISVE; and
Building Decontamination
Capital Cost:	$1,008,000
Annual Operation and Maintenance Cost: $824,000
Present-Worth Cost:	$2,383,000
Construction Time:	6 months
This alternative includes the excavation of all VOC-, SVOC-,
and metal-contaminated surface soils which exceed the
TAGM objectives, the trench and sumps inside the building,
and the drywells. In addition, the building floor would be
decontaminated as in Alternative SC-2.
The estimated volume of contaminated soil to be excavated
is 270 cubic yards. Excavation of the surface soil, sumps,
and building trench would be to approximately two feet. The
actual extent of the excavation and the volume of the
EPA Region II - July 2004
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Superfund Proposed Plan
Jackson Steel Site
excavated material would be based on post-excavation
confirmatory sampling.
Underthis alternative, the VOC-contaminated soils would be
remediated by ISVE. Under this treatment process, air
would be forced through a series of wells to volatilize the
solvents contaminating the soils in the unsaturated zone
(above the water table). The extracted vapors would be
treated by granular activated carbon and/or other
appropriate technologies before being vented to the
atmosphere. The exact configuration and number of
vacuum extraction wells would be determined during the
remedial design.
While the actual period of operation of the ISVE system
would be based upon soil sampling results which
demonstrate that the affected soils have been treated to soil
TAGM objectives and indoor air VOC levels in the adjacent
affected buildings have been reduced to acceptable health
levels with the subslab vacuum extraction system turned off,
it is estimated that the system would operate for a period of
two years. Should the former daycare center or former
billiards parlor buildings be occupied during the course of
the remediation, monitoring to assure that no unacceptable
vapor exposure takes place would be instituted, and the
ventilation system installed during the Rl would be
appropriately maintained.
The excavated areas would be backfilled with clean fill and
the previously paved areas would be re-paved. All
excavated material would be characterized and transported
fortreatment and/or disposal at an off-site RCRA-compliant
facility.
Groundwater Remedial Alternatives
be reviewed at least once every five years. If justified by the
review, remedial actions may be implemented to remove or
treat the wastes.
Alternative GW-1: No Action
Capital Cost:
Annual Monitoring Operation and
Maintenance Cost:
Present-Worth Cost:
Construction Time:
$0
$0
$0
0 months
Alternative GW-2: Groundwater Extraction
Treatment for Upper and Lower Aquifers
and
Capital Cost:
Annual Operation, Maintenance,
and Monitoring Cost:
Present-Worth Cost:
Construction Time:
$2,476,000-
$3,029,000
$682,000-
$727,000
$6,387,000-
$6,652,000
6 months
Under this alternative, four groundwater extraction wells
would be installed in the Upper Glacial Aquifer in the source
area. In consultation with NYSDEC, the extent of the off-
site groundwater contamination and its potential impact on
the public water supply wells would be determined during
the remedial design phase. Based on the evaluation of off-
site groundwater data that would be collected, if it is
determined that site-related contamination is affecting the
aquifers, this alternative would be expanded, as necessary,
to include the off-site groundwater contamination and its
potential impacts on the public water supply wells.
The extracted water would be treated at an on-site facility by
air stripping, carbon adsorption, and methods appropriate
for the treatment of metals. The treated water would be
reinjected into the aquifer.
Airstripping involves pumping untreated groundwatertothe
top of a "packed" column, which contains a specified amount
of inert packing material. The column receives ambient air
under pressure in an upward direction from the bottom of
the column as the water flows downward, transferring VOCs
to the air phase. The air-stripping process would be
followed by a groundwater polishing system using granular
activated carbon and/or other appropriate technologies. To
comply with New York State air guidelines, granular
activated carbon treatment of the air strippers' air exhaust
streams may be necessary.
The Superfund program requires that the "no-action"
alternative be considered as a baseline for comparison with
the other alternatives. The no-action remedial alternative
would not include any physical remedial measures to
address the groundwater contamination at the site.
Based on groundwater modeling, it has been estimated that
it would take 12 years for the groundwater in the upper and
lower aquifers to be restored to drinking water quality
through dispersion, dilution and volatilization.
Because this alternative would result in contaminants
remaining on-site above levels that allow for unrestricted
use and unlimited exposure, CERCLA requires that the site
In consultation with NYSDEC, the extent of the off-site
groundwater contamination and its potential impact on the
public water supply wells would be determined during the
remedial design phase. Based on the evaluation of off-site
groundwater data that would be collected, if it is determined
that site-related contamination is affecting the aquifer, this
alternative would be expanded, as necessary, to include the
off-site groundwater contamination and its potential impacts
on the public water supply wells.Because this alternative
would result in contaminants remaining on-site above levels
that allow for unrestricted use and unlimited exposure,
CERCLA requires that the site be reviewed at least once
every five years.
EPA Region II - July 2004
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Jackson Steel Site
Alternative GW-3: In-Situ Chemical Oxidation for
Treatment of Upper Aquiferand Groundwater Extraction
and Treatment for Lower Aquifer
Capital Cost:
Annual Operation, Maintenance
and Monitoring Cost:
Present-Worth Cost:
Construction Time:
$1,750,000-
$2,303,000
$413,000-
$458,000
$4,159,000-
$4,425,000
6 months
This alternative is the same as Alternative GW-2, except
instead of extracting contaminated groundwater from the
Upper Glacial Aquifer, an oxidizing agent7, such as
potassium permanganate (KMn04) or hydrogen peroxide
(H202), would be injected via approximately 12 wells
installed in the Upper Glacial Aquifer in the source area.
Under this process, the oxidizing agent would chemically
transform the VOCs into less toxic compounds or to carbon
dioxide, and water. Bench- and pilot-scale treatability
studies would be performed to optimize the effectiveness of
the injection system and to determine optimum oxidant
delivery rates and locations for the injection-well points.
Based on the evaluation of off-site groundwater data that
would be collected, if it is determined that site-related
contamination is affecting the aquifer, this alternative would
be expanded, as necessary, to include the off-site
groundwater contamination and its potential impacts on the
public water supply wells.
Because this alternative would result in contaminants
remaining on-site above levels that allow for unrestricted
use and unlimited exposure, CERCLA requires that the site
be reviewed at least once every five years.
Alternative GW-4: In-Situ Air Sparging for Treatment of
Upper Aquifer and Groundwater Extraction and
Treatment for Lower Aquifer
Capital Cost:
Annual Operation, Maintenance, and
Monitoring Cost:
Present-Worth Cost:
Construction Time:
$1,189,000-
$1,742,000
$673,500-
$718,500
$4,168,000-
$4,433,000
6 months
This alternative is the same as Alternative GW-2, except
instead of extracting contaminated groundwater from the
Upper Glacial Aquifer, it would be treated with air sparging.
Air sparging involves injecting air, under pressure, into the
aquifer via injection wells. Under this process, bubbles are
An oxidizing agent uses oxygen to degrade VOCs.
EPA Region II - July 2004
formed from the injected and air, which strip the VOCs from
the groundwater. A vapor extraction system would be used
to remove the generated vapors.
Based on the evaluation of off-site groundwater data that
would be collected, if it is determined that site-related
contamination is affecting the aquifer, this alternative would
be expanded, as necessary, to include the off-site
groundwater contamination and its potential impacts on the
public water supply wells.
Based on groundwater modeling, it has been estimated that
it would take two years to remediate the upper aquifer and
eight years for the groundwater in the lower aquifer to be
restored to drinking water quality (six years if both on-site
and off-site groundwater extraction wells are used) under
this alternative.
Because this alternative would result in contaminants
remaining on-site above levels that allow for unrestricted
use and unlimited exposure, CERCLA requires that the site
be reviewed at least once every five years.
COMPARATIVE ANALYSIS OF ALTERNATIVES
During the detailed evaluation of remedial alternatives, each
alternative is assessed against nine evaluation criteria,
namely, overall protection of human health and the envi-
ronment, compliance with applicable or relevant and
appropriate requirements, long-term effectiveness and
permanence, reduction of toxicity, mobility, or volume
through treatment, short-term effectiveness,
implementability, cost, and state and community
acceptance.
The evaluation criteria are described below.
Overall protection of human health and the
environment addresses whether or not a remedy
provides adequate protection and describes how
risks posed through each exposure pathway (based
on a reasonable maximum exposure scenario) are
eliminated, reduced, or controlled through treat-
ment, engineering controls, or institutional controls.
Compliance with ARARs addresses whether or not
a remedy would meet all of the applicable or
relevant and appropriate requirements of other
federal and state environmental statutes and
requirements or provide grounds for invoking a
waiver.
Long-term effectiveness and permanence refers to
the ability of a remedy to maintain reliable protec-
tion of human health and the environment over
time, once cleanup goals have been met. It also
addresses the magnitude and effectiveness of the
measures that may be required to manage the risk
posed by treatment residuals and/or untreated
wastes.
Reduction of toxicity, mobility, or volume through
treatment is the anticipated performance of the
treatment technologies, with respect to these
parameters, a remedy may employ.
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Short-term effectiveness addresses the period of
time needed to achieve protection and any adverse
impacts on human health and the environment that
may be posed during the construction and im-
plementation period until cleanup goals are
achieved.
Implementabilitv is the technical and administrative
feasibility of a remedy, including the availability of
materials and services needed to implement a
particular option.
Cost includes estimated capital and operation and
maintenance costs, and net present-worth costs.
State acceptance indicates if, based on its review of
the RI/FS and Proposed Plan, the state concurs
with the preferred remedy at the present time.
Community acceptance will be assessed in the
ROD and refers to the public's general response to
the alternatives described in the Proposed Plan and
the RI/FS reports.
A comparative analysis ofthese alternatives based upon the
evaluation criteria noted above follows.
Overall Protection of Human Health and the Environment
Alternative SC-1 (no action) would not be protective of
human health and the environment, since it would not
actively address the contaminated soils, which present
unacceptable risks of exposure and are a source of
groundwater contamination. Alternative SC-2 (excavation
of contaminated soils down to the watertable, contents of
the dry wells, and trench, and off-site treatment/disposal),
and Alternative SC-3 (excavation of contaminated surface
soils, contents of the dry wells, and trench, and off-site
treatment/disposal, and ISVE for subsurface contaminated
soils) would be protective of human health and the
environment, since each alternative relies upon a remedial
strategy and/or treatment technology capable of eliminating
human exposure and removing the source of groundwater
contamination in the unsaturated zone. Under these
alternatives, the contaminants would either be treated
on-property or treated/disposed of off-site.
Alternative GW-1 (no action) would be the least protective
groundwater alternative in that it would result in no active
measures to restore groundwater quality to drinking water
standards. Based on hydrogeological modeling presented
in Appendix G of the FS report, the contaminant mass is
projected to decrease over time, as contaminated
groundwater migrates. Under this alternative, the
restoration of the groundwater would take a longer time (an
estimated 12 years) in comparison to the other alternatives.
All three of the active groundwater alternatives are
estimated to restore groundwaterquality in the loweraquifer
in 8 years and, therefore, would be protective of human
health and the environment. The restoration of the upper
aquifer, which is more likely to affect soil vapor content of
the overlying soils, is achieved at distinct time frames forthe
three groundwater treatment alternatives. Specifically, for
Alternative GW-3 (in-situ chemical oxidation fortreatment of
upper aquifer and groundwater extraction and treatment for
lower aquifer), the upper aquifer is anticipated to be cleaned
in one month. This time-frame is much faster than for
Alternative GW-3 (groundwater extraction and treatment for
upper and lower aquifers) and Alternative GW-4 (in-situ air
sparging for treatment of upper aquifer and groundwater
extraction and treatment for lower aquifer) for which the
cleanup time-frames are five and two years respectively.
Therefore, in terms of reducing soil vapors emanating from
the upper aquifer, Alternative GW-3 would be the most
protective of human health and the environment.
Compliance with ARARs
There are currently no federal or state promulgated
standards for contaminant levels in soils, only New York
State soil cleanup objectives as specified in the soil TAGM
(which are used as "To-Be-Considered" criteria).
Since the contaminated soils would not be addressed under
Alternative SC-1 (no action), this alternative would not
comply with the soil cleanup objectives. Alternative SC-2
(excavation of contaminated soils down to the watertable,
contents of the dry wells, sumps, and trench, and off-site
treatment/disposal), and Alternative SC-3 (excavation of
contaminated surface soils, contents of the dry wells,
sumps, and trench, and off-site treatment/disposal, and
ISVE for subsurface contaminated soils) would attain the
soil cleanup objectives specified in the TAGM.
Alternative SC-2 and Alternative SC-3 would be subject to
New York State and federal regulations related to the
transportation and off-site treatment/disposal of wastes.
Alternatives SC-2 and SC-3 would involve the excavation of
contaminated soils and would, therefore, require compliance
with fugitive dust and VOC emission regulations. In the
case of Alternative SC-3, compliance with air emission
standards would be required forthe ISVE system, as well.
Specifically, treatment of off-gases would have to meet the
substantive requirements of New York State Regulations for
Prevention and Control of Air Contamination and Air
Pollution (6 NYCRR Part 200 et.seq.) and comply with the
substantive requirements of other state and federal air
emission standards.
EPA and NYSDOH have promulgated health-based
protective MCLs (40 CFR Part 141, and 10 NYCRR,
Chapter 1), which are enforceable standards for various
drinking water contaminants (chemical-specific ARARs).
The aquifer is classified as Class GA (6 NYCRR 701.18),
meaning that it is designated as a potable water supply.
Although the groundwater at the site is not presently being
utilized as a potable water source, achieving MCLs in the
groundwater is an applicable standard, because area
groundwater is a source of drinking water.
Alternative GW-1 does not provide for any direct
remediation of the groundwater and would, therefore,
involve no actions to achieve chemical-specific ARARs. All
three of the active groundwater alternatives would be
effective in reducing groundwater contaminant
concentrations to below MCLs.
Any emissions from the air stripper under Alternatives GW-
2, GW-3, and GW-4 would be required to comply with the
substantive requirements of state and federal air emission
standards.
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Long-Term Effectiveness and Permanence
Alternative SC-1 would involve no active remedial measures
and, therefore, would not be effective in eliminating the
potential exposure to contaminants in soil and would allow
the continued migration of contaminants from the soil to the
groundwater. Alternative SC-2 and Alternative SC-3 would
both be effective in the long term and would provide
permanent remediation by either removing the contaminated
soils from the site or treating them on-site.
Alternative SC-3 would generate treatment residuals which
would have to be appropriately handled.
Alternative GW-1 would be the least effective in the long
term in restoring groundwater quality, since it would take an
estimated 12 years to restore groundwater. Alternatives
GW-2, GW-3, and GW-4 would effectively restore
groundwater quality in an estimated eight years (six years if
both on-site and off-site groundwater extraction wells are
used).
Alternatives GW-2, GW-3, and GW-4 may generate
treatment residuals which would have to be appropriately
handled.
Reduction in Toxicity, Mobility, or Volume Through
Treatment
Alternative SC-1 would provide no reduction in toxicity,
mobility or volume. Under Alternative SC-2, the toxicity,
mobility, and volume of the contaminants would be
eliminated by removing the contaminated soil from the
property for treatment/disposal. Under Alternative SC-3 the
toxicity, mobility, and volume of contaminants would be
reduced or eliminated through on-site treatment and by
removing the contaminated soil from the property for
treatment/disposal.
Alternative GW-1 would not effectively reduce the toxicity,
mobility, or volume of contaminants in the groundwater, as
this alternative involves no active remedial measures.
Alternatives GW-2, GW-3, and GW-4 would reduce the
toxicity, mobility, or volume of contaminants in the
groundwater through treatment at the source, thereby
satisfying CERCLA's preference for treatment.
Short-Term Effectiveness
Alternative SC-1 does not include any physical construction
measures in any areas of contamination and, therefore,
would not present any potential adverse impacts to on-
property workers or the community as a result of its
implementation. Alternatives SC-2 and SC-3 could present
some limited adverse impacts to on-site workers through
dermal contact and inhalation related to excavation
activities. Alternative SC-3 could also result in some
adverse impacts to on-site workers through dermal contact
and inhalation related to the installation of ISVE wells
through contaminated soils. Noise from the excavation work
and from the treatment unit associated with Alternatives SC-
2 and SC-3 could present some limited adverse impacts to
on-site workers and nearby residents. In addition, interim
and post-remediation soil sampling activities would pose
some risk. The risks to on-site workers and nearby
residents under all of the alternatives could, however, be
mitigated by following appropriate health and safety
EPA Region II - July 2004
protocols, by exercising sound engineering practices, and by
utilizing proper protective equipment.
Alternative SC-2 would require the off-site transport of a
significant volume of contaminated soil, which may pose the
potential for traffic accidents, which in turn could result in
releases of hazardous substances. Alternative SC-3 would
also require the off-site transport of contaminated soil, but at
a volume substantially less than Alternative SC-2.
Under Alternative SC-2, substantial disturbance of the land
during excavation activities could affect the surface water
hydrology of the property. For Alternatives SC-2 and SC-3,
there is a potential for increased stormwater runoff and
erosion during excavation and construction activities that
would have to be properly managed to prevent or minimize
any adverse impacts. For these alternatives, appropriate
measures would have to be taken during excavation
activities to prevent transport of fugitive dust and exposure
of workers and downgradient receptors to VOCs.
Since no actions would be performed under Alternative SC-
1, there would be no implementation time. It is estimated
that it would take six months to excavate and transport the
contaminated soils, contents of the dry wells, and trench
contents to an EPA-approved treatment/disposal facility
under Alternative SC-2. It is estimated that Alternative SC-3
would require six months to excavate and transport the
contaminated surface soils, contents of the dry wells,
sumps, and trench to an EPA-approved treatment/disposal
facility and to install the ISVE system and two years to
achieve the soil cleanup objectives.
All of the action groundwater alternatives could present
some limited adverse short-term impacts to on-site workers
through dermal contact and inhalation related to
groundwater sampling activities. Alternative GW-2,
Alternative GW-3, and Alternative GW-4 could present
adverse impacts to on-site workers, since these alternatives
would involve the installation of groundwater extraction, air
sparging, and/or oxidation agent injection wells through
potentially contaminated soils and groundwater. Alternative
GW-3 could pose more adverse impacts than Alternatives
GW-2 and GW-4, since it would require the installation of
significantly more well points than Alternatives GW-2 and
GW-4. Noise from the treatment units associated with
Alternatives GW-2, GW-3, and GW-4 could present some
limited adverse impacts to on-site workers and nearby
residents. The risks to on-site workers and nearby residents
underall ofthe alternatives could, however, be minimized by
following appropriate health and safety protocols, by
exercising sound engineering practices, and by utilizing
proper protective equipment.
Since no activities would be performed under Alternative
GW-1, no time would be required to implement this
alternative. It is estimated that the groundwater remediation
systems under Alternative GW-2, Alternative GW-3, and
Alternative GW-4 would be constructed in six months.
Based on groundwater modeling, it has been estimated that
it would take 12 years for the groundwater in the upper and
lower aquifers to be restored to drinking water quality
through dispersion, dilution and volatilization under
Alternative GW-1. Alternatives GW-2, GW-3, and GW-4,
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Jackson Steel Site
with similar configurations with respect to the lower aquifer,
would all require approximately eight years to remediate the
lower aquifer (six years if both on-site and off-site
groundwater extraction wells are used). With varying
technologies, Alternatives GW-2, GW-3, and GW-4 would
require an estimated 5 years, 1 month, and two years,
respectively, to remediate the upper aquifer. The actual time
for the groundwater to be remediated under all of the
alternatives may vary and may need to be refined based on
the results of groundwater monitoring and, as appropriate,
groundwater modeling.
Implementabilitv
Alternative SC-1 would be the easiest to implement, as
there are no activities to undertake. Potentially difficult
factors related to the excavation of soils down to fifty feet
bgs adjacent to the on-site building and on a property that is
so small may need to be resolved for Alternative SC-2 .
Alternative SC-3 would be much easier to implement than
Alternative SC-2, since large-scale soil excavation and
handling would not be required. Also, because of space
limitations, staging the excavated soil for off-site
treatment/disposal under Alternative SC-2 may prove
difficult.
Both soil action alternatives would employ technologies
known to be reliable and that can be readily implemented.
In addition, equipment, services, and materials needed for
these alternatives are readily available, and the actions
underthese alternatives would be administratively feasible.
Sufficient facilities are available forthe treatment/disposal of
the excavated materials under Alternatives SC-2 and SC-3.
Under Alternatives SC-2 and SC-3, determining the extent
of the excavation could be easily accomplished through
post-excavation soil sampling and analysis. Monitoring the
effectiveness of the ISVE system under Alternative SC-3
would be easily accomplished through soil and soil-vapor
sampling and analysis.
Alternative GW-1 would be the easiest to implement, since
it would not entail the performance of any activities. The in-
situ chemical oxidation and the air sparging systems forthe
upper aquifer under Alternative GW-3, and GW-4,
respectively, and groundwater extraction and treatment
systems under Alternatives GW-2, GW-3, and GW-4 would
be relatively easy to implement. For Alternative GW-3, the
oxidant application rate and the rate of the oxidation reaction
would need to be carefully monitored and adjusted, as
needed, during implementation to ensure that the oxidants
do not reach the municipal water supply wells and that the
amount of heat and gases generated during the application
of the oxidants are properly controlled.
Air sparging, as a general rule, is only effective to a depth of
fifty feet below the water table. At the site, the saturated
thickness of the upper aquifer plume is more than one
hundred feet. Consequently, bench- and pilot-scale
treatability studies would be required to verify its
effectiveness. Bench and pilot-scale treatability studies
would also be required to verify the effectiveness of the in-
situ chemical oxidation system.
The groundwater extraction and treatment system that
would be used under all three treatment alternatives has
been implemented successfully at numerous sites to extract,
treat, and hydraulically control contaminated groundwater.
Extracting contaminated groundwaterfromthe loweraquifer
in off-site areas would, however, be more difficult to
implement than extracting contaminated groundwater from
the lower aquifer in on-site areas. While there is sufficient
space on the property for most of the constructed
components of each of the active groundwater alternatives,
if off-site groundwater extraction and treatment were
required, it would necessitate the installation of piping and
other components in the street right-of-way, potentially
complicated by the presence of utilities; it would also affect
traffic during construction.
The airstripping and granular activated carbon technologies
that would be used for groundwater treatment in all three
alternatives are proven and reliable in achieving the
specified performance goals and are readily available.
Cost
The present-worth cost associated with Alternative SC-3 is
calculated using a discount rate of 3.2% and a 2-year time
interval. The present-worth costs associated with the lower
aquifer components of the groundwater alternatives are
calculated using the same discount rate and an eight-year
time interval for the action alternatives if only on-site
groundwater extraction wells are used and a six-year time
interval if both on-site and off-site groundwater extraction
wells are used. The present-worth costs associated with the
upper aquifer components of the groundwater alternatives
are calculated using a discount rate of 3.2% and five-year
and two-yeartime frames, respectively, for Alternative GW-2
and Alternative GW-4. Although the time required to
implement Alternative GW-3 (in-situ chemical oxidation for
treatment of upper aquifer and groundwater extraction and
treatment for lower aquifer) is less than a year, the present-
worth costs were calculated using a five-year time interval
to allow for additional testing and treatment should a
reoccurrence of contaminants occur.
The estimated capital, operation, maintenance, and
monitoring (OM&M), and present-worth costs for each of the
alternatives are presented below.
Alternative
SC-1
SC-2
SC-3
GW-1
GW-2
GW-3
GW-4
Capital
$0
$5,299,000
$1,008,000
$0
$2,476,000-
$3,029,000
$1,750,000-
$2,303,000
$1,189,000-
$1,742,000
Annual OM&M
$0
$0
$824,000
$0
$682,000-
$727,000
$413,000-
$458,000
$673,500-
$718,500
Total
Present-
Worth
$0
$5,299,000
$2,383,000
$0
$6,387,000-
$6,652,000
$4,159,000-
$4,425,000
$4,168,000-
$4,433,000
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Jackson Steel Site
As can be seen by the cost estimates, Alternative SC-1 is
the least costly soil alternative at $0. Alternative SC-2 is the
most costly soil alternative at $5,299,000. The least costly
groundwater remedy is Alternative GW-1 at $0. Alternative
GW-2 is the most costly groundwater alternative estimated
to range from $6,387,000-6,652,000, depending on whether
groundwater from the lower aquifer is extracted only from
on-site wells (lower cost) or from both on-site and off-site
wells (higher cost.)
State Acceptance
NYSDEC concurs with the preferred source control and
groundwater alternatives.
Community Acceptance
Community acceptance of the preferred alternative will be
assessed in the ROD following review of the public
comments received on the Proposed Plan.
PROPOSED REMEDY
Based upon an evaluation of the various alternatives, EPA
and NYSDEC recommend Alternative SC-3 (excavation of
contaminated surface soils, contents of the dry wells,
sumps, and trench, and off-site treatment/disposal, and
ISVE for subsurface contaminated soils) and Alternative
GW-3 (in-situ chemical oxidation for treatment of upper
aquifer and groundwater extraction and treatment for lower
aquifer) as the preferred remedy for soil and groundwater,
respectively. Specifically, this would involve the following:
Excavation of the contents of the dry wells, the
sumps and trench inside the building, and surface
soils contaminated with VOCs, SVOCs, pesticides
and metals. The estimated volume of the
contaminated soil to be excavated is 270 cubic
yards. Excavation of the surface soil, sumps, and
building trench would be to approximately two feet.
Confirmatory sampling would be conducted to
ensure that all soils above the cleanup objectives
have been removed. The excavated areas would
be backfilled with clean fill and the previously paved
areas would be re-paved. All excavated material
would be characterized and transported for
treatment and/or disposal at an off-site RCRA-
compliant facility.
Treatment of the VOC-contaminated unsaturated
soils using ISVE in on-site source areas and
underneath two adjacent affected buildings. The
extracted vapors would be treated by granular
activated carbon and/or other appropriate
technologies before being vented to the
atmosphere. Post-treatment confirmatory soil
samples would be collected to ensure that the
entire source area has been effectively treated to
the cleanup objectives. Should the former daycare
center or former billiards parlor buildings be
occupied during the course of the remediation,
monitoring to assure that no unacceptable vapor
exposure takes place would be instituted, and the
ventilation system installed during the Rl would be
appropriately maintained
Decontamination of the building floor through
vacuuming and powerwashing. All vacuumed dust
and wash water would be transported for treatment
and/or disposal at an off-site RCRA-compliant
facility.
In-situ treatment of the on-site contaminated
groundwater in the upper aquifer in the source area
by injection of an oxidizing agent, such as KMn04or
H202, via on-site injection wells. The oxidizing
agent would chemically transform the VOCs into
less toxic compounds or to carbon dioxide, and
water. The exact configuration and number of
injection wells would be determined during the
remedial design. The system would be operated
until MCLs are attained in the groundwater.
Collection of the contaminated groundwater in the
lower aquifer with extraction wells if confirmatory
sampling during the remedial design phase
indicates that the site is the source of the
contamination.
Treatment of the extracted groundwater at an on-
site facility by air stripping, carbon adsorption, and
methods appropriate for treatment of metals. The
treated water would be reinjected into the aquifer.
In consultation with NYSDEC, the extent of the off-
site groundwater contamination and its potential
impact on the public water supply wells would be
determined during the remedial design phase.
Based on the evaluation of off-site groundwater
data that would be collected, if it is determined that
site-related contamination is affecting the aquifer,
the proposed remedy would be expanded, as
necessary, to include the off-site groundwater
contamination and its potential impacts on the
public water supply wells.
Long-term groundwater monitoring in orderto verify
that the concentrations and the extent of
groundwater contaminants are declining, that the
remedies remain effective, and that public water
supplies are protected. The exact frequency and
parameters of sampling and the location of any
additional monitoring wells would be determined
during the design phase.
Bench- and pilot-scale treatability studies and groundwater
modeling would be performed to optimize the effectiveness
of the injection system and to determine optimum installation
locations for the injection-well points.
Because the preferred remedy would result in contaminants
remaining on-site above levels that allow for unrestricted
use and unlimited exposure, CERCLA requires that the site
be reviewed at least once every five years. If justified by the
review, additional remedial actions may be implemented.
Basis for the Remedy Preference
While Alternative SC-2 and Alternative SC-3, would both
effectively achieve the soil cleanup levels, Alternative SC-2
would be significantly more expensive than Alternative SC-
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Jackson Steel Site
3. In addition, potentially difficult factors related to the
excavation of soils down to fifty feet bgs adjacent to on-site
buildings, and to the staging of the excavated soil for off-site
treatment/disposal in such a limited area, would render
Alternative SC-2 more difficult to implement than Alternative
SC-3.
While Alternative SC-3 would take longerto achieve the soil
cleanup levels than Alternative SC-2 (an estimated two
years versus six months), considering that the groundwater
component of the preferred remedy would address the
contaminated groundwater in an estimated eight years, the
increase in the time needed to clean up the soil would not
be a significant concern. Therefore, EPA believes that
Alternative SC-3 would effectuate the soil cleanup while
providing the best balance of tradeoffs with respect to the
evaluating criteria.
All three of the active treatment groundwater alternatives are
estimated to take eight years to restore groundwater quality
in the lower aquifer. Restoration of the upper aquifer, which
is more likely to affect the soil vapor content of the overlying
soils, is estimated to be achieved in one month for the
preferred alternative, Alternative GW-3, whereas the time
needed for upper aquifer cleanup by Alternatives GW-2 and
GW-4 is five and two years, respectively. Finally, Alternative
GW-2 is approximately fifty percent greater than the cost of
Alternatives GW-3 and GW-4, which have similar costs.
Therefore, EPA has identified Alternative GW-3 as its
preferred groundwater alternative since it would effectuate
the groundwater cleanup while providing the best balance of
tradeoffs among the alternatives with respect to the
evaluation criteria.
The preferred remedy is believed to provide the greatest
protection of human health and the environment, provide the
greatest long-term effectiveness, be able to achieve the
ARARs more quickly, or as quickly, as the other alternatives,
and is cost-effective. Therefore, the preferred remedy will
provide the best balance of tradeoffs among alternatives
with respect to the evaluation criteria. EPA and NYSDEC
believe that the preferred remedy will treat principal threats,
be protective of human health and the environment, comply
with ARARs, be cost-effective, and utilize permanent
solutions and alternative treatmenttechnologies or resource
recovery technologies to the maximum extent practicable.
The preferred remedy also will meet the statutory preference
for the use of treatment as a principal element.
EPA Region II - July 2004
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